Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Neuronal loss in the cerebral cortex
8 0 7 0.32 0 0
Frontotemporal Dementia With Motor Neuron Disease
13 0 8 0.31 0 0
CUI: C4014650
Disease: Abnormal mitochondrial morphology
Abnormal mitochondrial morphology
13 0 8 0.31 0 0
Abnormal upper motor neuron morphology
20 0 9 0.28 0 0
Abnormal lower motor neuron morphology
23 0 9 0.26 0 0
CUI: C1720037
Disease: Supranuclear gaze palsy
Supranuclear gaze palsy
19 0 8 0.25 0 0
Fatigable weakness of swallowing muscles
39 0 11 0.22 0 0
CUI: C0234410
Disease: Physiologic disinhibition
Physiologic disinhibition
23 0 8 0.22 0 0
CUI: C0869474
Disease: Dyscalculia
Dyscalculia
20 0 7 0.21 0 0
Impaired vibration sensation in the lower limbs
39 0 10 0.20 0 0
Urinary bladder sphincter dysfunction
28 0 8 0.20 0 0
CUI: C0023066
Disease: Laryngospasm
Laryngospasm
48 0 11 0.19 0 0
CUI: C0221166
Disease: Paraparesis
Paraparesis
31 0 8 0.18 0 0
CUI: C0154682
Disease: Lateral Sclerosis
Lateral Sclerosis
19 0 6 0.18 0 0
CUI: C4553976
Disease: Urinary Urgency, CTCAE 5
Urinary Urgency, CTCAE 5
34 0 8 0.17 0 0
CUI: C0231687
Disease: Spastic gait
Spastic gait
62 0 12 0.17 0 0
CUI: C0043352
Disease: Xerostomia
Xerostomia
56 0 11 0.17 0 0
Primary Progressive Nonfluent Aphasia
21 0 6 0.17 0 0
CUI: C3711371
Disease: Spastic Paraplegia Type 4
Spastic Paraplegia Type 4
7 0 4 0.17 0 0
Behavioral variant of frontotemporal dementia
35 0 8 0.17 0 0
Fatigable weakness of respiratory muscles
60 0 11 0.16 0 0
CUI: C1846017
Disease: Progressive pes cavus
Progressive pes cavus
9 0 4 0.15 0 0
CUI: C0085606
Disease: Urgency of micturition
Urgency of micturition
40 0 8 0.15 0 0
Spastic paraplegia 4, autosomal dominant
10 0 4 0.15 0 0
Hereditary Autosomal Dominant Spastic Paraplegia
27 0 6 0.14 0 0